These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

150 related items for PubMed ID: 7802045

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. [Opitz-trigonocephaly syndrome--a characteristic dysmorphia-retardation syndrome of unclear origin].
    Choudhury AR, Renneberg A, Rackowitz A, Stephani U.
    Klin Padiatr; 1992; 204(3):171-3. PubMed ID: 1614184
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Multiple epiphyseal dysplasia with small head, congenital nystagmus, hypoplasia of corpus callosum, and leukonychia totalis: a variant of Lowry-Wood syndrome?
    Yamamoto T, Tohyama J, Koeda T, Maegaki Y, Takahashi Y.
    Am J Med Genet; 1995 Mar 13; 56(1):6-9. PubMed ID: 7747786
    [Abstract] [Full Text] [Related]

  • 6. [Pallister-Hall syndrome].
    Oho Y, Okuyama T.
    Ryoikibetsu Shokogun Shirizu; 2000 Mar 13; (30 Pt 5):23-5. PubMed ID: 11057130
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Craniosynostosis, agenesis of the corpus callosum, serve mental retardation, distinctive facies, camptodactyly, and hypogonadism.
    Lin AE, Gettig E.
    Am J Med Genet; 1990 Apr 13; 35(4):582-5. PubMed ID: 2333890
    [No Abstract] [Full Text] [Related]

  • 9. Micropenis in a newborn with acrocallosal syndrome.
    Ikbal M, Tastekin A, Ors R.
    Genet Couns; 2004 Apr 13; 15(2):233-5. PubMed ID: 15287426
    [No Abstract] [Full Text] [Related]

  • 10. Toriello-Carey syndrome with endocardial fibroelastosis.
    Ohta H, Masuno M, Kimura J, Imaizumi K, Kuroki Y, Yasui S, Aida N, Tanaka Y.
    Am J Med Genet; 1999 Nov 26; 87(3):271-2. PubMed ID: 10564885
    [No Abstract] [Full Text] [Related]

  • 11. Partial trisomy 13 with features similar to C syndrome.
    Phadke SR, Patil SJ.
    Indian Pediatr; 2004 Jun 26; 41(6):614-7. PubMed ID: 15235171
    [Abstract] [Full Text] [Related]

  • 12. Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: a new syndrome.
    Schinzel A, Schmid W.
    Am J Med Genet; 1980 Jun 26; 6(3):241-9. PubMed ID: 7424976
    [Abstract] [Full Text] [Related]

  • 13. Greig cephalopolysyndactyly syndrome with dysgenesis of the corpus callosum in a Bedouin family.
    Marafie MJ, Temtamy SA, Rajaram U, al-Awadi SA, el-Badramany MH, Farag TI.
    Am J Med Genet; 1996 Dec 18; 66(3):261-4. PubMed ID: 8985483
    [Abstract] [Full Text] [Related]

  • 14. GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome.
    Kang S, Graham JM, Olney AH, Biesecker LG.
    Nat Genet; 1997 Mar 18; 15(3):266-8. PubMed ID: 9054938
    [Abstract] [Full Text] [Related]

  • 15. Familial Pallister-Hall syndrome: case report and hormonal evaluation.
    Sills IN, Rapaport R, Robinson LP, Lieber C, Shih LY, Horlick MN, Schwartz M, Desposito F.
    Am J Med Genet; 1993 Sep 01; 47(3):321-5. PubMed ID: 8135274
    [Abstract] [Full Text] [Related]

  • 16. Heritable syndromes with hypothalamic hamartoma and seizures: using rare syndromes to understand more common disorders.
    Biesecker LG.
    Epileptic Disord; 2003 Dec 01; 5(4):235-8. PubMed ID: 14975792
    [Abstract] [Full Text] [Related]

  • 17. Hydrometrocolpos as a neonatal manifestation of the Bardet-Biedl syndrome.
    Mehrotra N, Taub S, Covert RF.
    Am J Med Genet; 1997 Mar 17; 69(2):220. PubMed ID: 9056566
    [No Abstract] [Full Text] [Related]

  • 18. Corpus callosum agenesis in Coffin-Lowry syndrome.
    Soekarman D, Fryns JP.
    Genet Couns; 1994 Mar 17; 5(1):77-80. PubMed ID: 8031540
    [Abstract] [Full Text] [Related]

  • 19. Pallister-Hall syndrome: clinical and MR features.
    Kuo JS, Casey SO, Thompson L, Truwit CL.
    AJNR Am J Neuroradiol; 1999 Mar 17; 20(10):1839-41. PubMed ID: 10588106
    [Abstract] [Full Text] [Related]

  • 20. An additional manifestation in acrocallosal syndrome: temporal lobe hypoplasia.
    Aykut A, Cogulu O, Ekmekci AY, Ozkinay F.
    Genet Couns; 2008 Mar 17; 19(2):237-40. PubMed ID: 18618999
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.